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Structure of 131666-74-5
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Methyl 2-(1H-indazol-3-yl)acetate features a rigid indazole core linked to an ester-functionalized side chain, enabling direct integration into diverse heterocyclic architectures. This bench-stable, moisture-tolerant reagent facilitates efficient coupling reactions and serves as a key scaffold for medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.
Methyl 2-(1H-indazol-3-yl)acetate serves as a versatile building block for indazole-based pharmaceutical intermediates, enabling efficient functionalization at the C3 position. Its ester group facilitates subsequent transformations such as hydrolysis, reduction, or coupling reactions, while the indazole core provides a rigid, bioactive scaffold. The compound exhibits good bench stability and is compatible with standard synthetic protocols, supporting its use in medicinal chemistry campaigns targeting kinase inhibitors and CNS modulators.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: